Dosage & Administration
Store below 110°F Avoid direct sunlight,fluorescent lighting, heat, and moisture.
Hand Sanitizer
FDA Label NDC 59004-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jacent Strategic Merchandising, Llc for the product Hand Sanitizer (NDC 59004-012). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Pure Water, Carbomer U21 (C10-30 Alkanol acrylate cros-inked polymer), Glycerin, Aloe extract,Chamomile Scent, Triethanolamine.
Indications & Usage
1.Adults and children over 2 years: Supervise children when they use this product
2.For occasional and personal domestic use.
3.Rub thoroughly into hands for at least 30 seconds. Allow to dry.
Otc - Active Ingredient
Ethyl Alcohol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
Warnings
1.For external use only
2.When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
3.Stop use and ask / consult a doctor / physician 1 health care practitioner I health care provider/ health care professional if iritation develops.
4.Keep out of reach of children.If swallowed, call a poison control centre or get medical help right away,
Package Label.Principal Display Panel
Label (Label)
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